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19 April 2021 - Late treatment study
Favipiravir Observational Study Interim Report 3
Favipiravir Observational Study Group, Fujita Health University (Preprint)
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Retrospective analysis of favipiravir use in 10,986 hospitalized patients, including analysis of changes in clinical status and side effects. Common adverse events were uric acid level increase and liver function enzyme increase. Authors note that early embryonic lethality and teratogenicity due to favipiravir have been observed in animal models, that pregnant women must be excluded, and that all patients and partners should practice effective contraception.
Favipiravir Observational Study Group et al., 4/19/2021, preprint, 1 author.
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